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A Message to Pharma CIOs: Optimizing Salesforce Improves Security and Compliance

pharmaphorum

However, issues like compliance, governance and security often are. That’s why CIOs and CTOs working within the life sciences industry need to include Salesforce org management as a key component of their standard operating procedures. This will help ensure consistency and compliance across the entire enterprise. .

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How AI/ML-based PHI & PII redaction solutions can help life sciences organizations

Cloudbyz

In today’s digital age, life sciences organizations are collecting, storing, and processing vast amounts of sensitive data, including personally identifiable information (PII) and protected health information (PHI). As such, it’s becoming increasingly challenging for organizations to manage and secure this data.

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Expert Insights: Development and Manufacture of Highly Potent Oral Liquids

XTalks

Best practices include the use of contained engineering solutions to safeguard drug product integrity and protect operators. These vulnerabilities necessitate robust preservation or sterilization measures to maintain product integrity throughout the shelf life.

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Is the proposed Data Protection and Digital Information Bill fit for purpose?

pharmaphorum

Instead, organisations will designate a senior employee to oversee an organisation’s compliance with data protection rules. It contains my own views and opinions and doesn’t constitute legal advice. Wendy Lloyd Godwin is the founder of Life Science Law. This Article is for information purposes only. About the author.

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Data protection upheld for subsequently approved combination drugs containing new chemical entities: Federal Court finds Minister of Health’s decision to deny generic ANDS filing is reasonable

Pharma in Brief

The Decision refused to accept Natco’s ANDS filing using Gilead Sciences Canada Inc.’s DESCOVY contains a combination of tenofovir alafenamide ( TAF ) hemifumarate and emtricitabine. Because DESCOVY contains TAF, it benefits from the same data protection term granted to GENVOYA. Background. Minister of Health’s Decision.

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Proposed amendments to the PM(NOC) Regulations: Patents claiming different salt forms of medicinal ingredients eligible for inclusion on the Patent Register

Pharma in Brief

As previously reported , the Proposed FDR Amendments were intended to clarify the regulatory requirements under the Abbreviated New Drug Submission (“ ANDS ”) pathway for generic drug products that contain different forms (e.g., different salt forms) of the medicinal ingredient in comparison to the Canadian Reference Product (“ CRP ”).

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Packaging Solutions for Pharmaceuticals & Medical Devices: Insights and Considerations

XTalks

A container closure system consists of all the packaging components that contain and protect a pharmaceutical product. Container Closure Systems. A container closure system protects the product from environmental conditions, safeguarding a product’s purity, strength, safety and efficacy.